Disease #01596 (CMH1 (cardiomyopathy, hypertrophic, familial, type 1), OMIM:192600)
Official abbreviation |
CMH1 |
Name |
cardiomyopathy, hypertrophic, familial, type 1 |
OMIM ID |
192600 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant, Digenic dominant |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
1 |
Associated with 3 genes |
CAV3, MYH7, MYLK2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2023-10-01 20:50:48 +02:00 (CEST) |
Individuals
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